Clinical Research Coordinator

About the position

We are seeking a dedicated Clinical Research Coordinator to join our team at TriHealth Hatton. The role involves coordinating and managing all components necessary for the successful participation and completion of clinical research trials. Acting as an educator, consultant/liaison, and evaluator, you will ensure clinical trials are conducted with safety, integrity, and efficiency, applying good clinical practices. Key responsibilities include coordinating Phase II-IV trials, from initial sponsor contact for site selection to study preparation, execution, and close-out. You will also be responsible for marketing and networking with sponsors, determining protocol feasibility, and addressing some budgetary issues. Adherence to the standard operating procedures of the TriHealth Hatton Research Institute is essential. Location: This position is based at GSH Hatton Institute and requires travel to all infusion locations within the TriHealth network.

Responsibilities

• Develop processes to facilitate the implementation of research protocols to ensure effective and safe medical research for all subjects.
• Coordinate necessary activities between Study Coordinators and the Principal Investigator.
• Perform initial and ongoing evaluations of research subjects and implement care aimed at achieving optimal outcomes.
• Ensure compliance with IRB/FDA standards and deadlines in study submissions, subject randomization and enrollment, progress reports, and reporting of deaths and adverse events.
• Assess potential subjects for inclusion and exclusion criteria.
• Maintain complete and thorough Case Report Forms in accordance with IRB and FDA standards.
• Support hospital staff in complying with research protocols, minimizing impact on their workload.
• Demonstrate knowledge of available studies, screen potential patients for eligibility, and guide physicians and staff in capturing protocol-related data points.
• Act as the point person for audit staff during institutional reviews, preparing written responses with plans of action for any deficiencies.

Requirements

• Bachelor's Degree in Biological Science; Hard Sciences, Psychology, or Sociology (Equivalent experience accepted in lieu of degree).
• Basic Life Support for Healthcare Providers (BLS) certification.
• Clinical Research experience preferred.

Benefits

• Full-time, Monday - Friday, Day shift.